Method and computer program product for distinguishing and sorting seeds containing a genetic element of interest

ABSTRACT

Seeds containing a genetic element of interest can be distinguished and sorted from a bulk sample of seeds. In certain embodiments, a marker is associated with at least some of the seeds containing a genetic element of interest, the seeds are excited using an photonic emitting device, and at least some of the seeds of the bulk sample are evaluated for the presence or absence of the marker and may be sorted based on the presence or absence of the marker. In certain embodiments, the marker is a red fluorescent protein marker. In certain embodiments, the red fluorescent protein marker is discernable when excited by a certain energy and the evaluating step comprises exciting the seeds containing a genetic element of interest with the certain energy and detecting an emission resulting at least in part from the exciting step.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of pending U.S. patentapplication Ser. No. 13/870,612, filed Apr. 25, 2013 which is acontinuation of Application Ser. No. 12/500,847, filed on Jul. 10, 2009,now U.S. Pat. No. 8,452,445, which is a continuation-in-part of U.S.patent application Ser. No. 12/108,198, filed on Apr. 23, 2008, now U.S.Pat. No. 8,626,337, which claims priority from U.S. ProvisionalApplication No. 60/913,562, filed on Apr. 24, 2007, each of which ishereby incorporated herein in its entirety by reference.

FIELD OF THE INVENTION

The various embodiments of the present invention relate generally to amethod and computer program product for distinguishing and sorting seedsthat contain genetic elements of interest from seeds that do not. Morespecifically, embodiments of the present invention are capable ofdistinguishing and sorting the seeds containing the genetic elements ofinterest by detecting the presence of one or more discernable markersthat are linked to one or more corresponding genetic elements ofinterest.

BACKGROUND OF THE INVENTION

Genetic engineering involves inserting new genetic information intoexisting cells of an organism to create a new genotype in order tomodify the organism for the purpose of changing one or more of itscharacteristics. A living organism may be genetically engineered for avariety of reasons, including incorporating novel and/or beneficialtraits into the organism. With regard to crop plants, this may includegenetically engineering seeds so that plants that grow from the seedsinclude one or more beneficial traits. Such genetic engineering mayinclude, but is not limited to, inserting genes encoding a discernablemarker or genes conferring resistance to herbicidal compounds. Theprogeny of individual genetically modified organisms may also contain agenetic element of interest such that researchers may wish to segregateand/or identify organisms (including seeds) that contain such geneticelements of interest from a bulk sample.

Conventional genetic techniques may also be used to combine traits fromat least two organisms to produce novel and/or beneficial traits in a“genetic cross” and/or hybrid organism.

It is often difficult to determine whether a particular seed contains agenetic element of interest, especially when mixed with seeds that havenot been so modified. Using previous techniques, a particular seed wouldhave to be germinated and then the resulting plant sampled to determinewhether the seed might contain the genetic element of interest.Alternatively, the seed itself would have to be sampled.

There are advantages, however, in distinguishing a set of seedscontaining a genetic element of interest before the respective plantsare germinated, especially in the plant research discipline, whereresearch plot space, personnel for sorting, and time are often limited.In maize and other wind-pollinated crops, plants are frequentlyhand-pollinated, wherein pollen is manually transferred from the tasselto the silk, and the silk is covered by a shoot bag to preventpollinated by other plants. This hand pollination process requiressignificant labor and a tassel bag and shoot bag. The prior eliminationof undesired plants (i.e. plants that do not contain a genetic elementof interest) by sorting seed may eliminate the need for this labor andtime-intensive activity. Additionally, researchers may be interested inthe yield potential of the plants germinated from seeds containing thegenetic element of interest. Thus, it is important that astatistically-significant number of plants germinate from seedscontaining the genetic element of interest in a defined space (i.e. aresearch plot). Furthermore, researchers desire accuracy and oftencannot afford to wait or guess to determine whether plants contain aparticular genetic element of interest. Additionally, seed and/or seedtissue sampling is a delicate art. For example, if too much tissue isremoved from a particular seed for sampling, there is a risk that theseed may not germinate or produce a viable plant.

Various local, federal, and international regulatory bodies require ahigh degree of accuracy with respect to the composition of seeds. Forexample, many regulatory bodies have established seed purity standardsthat require a “zero-tolerance” policy with regard to seed composition.In such a manner, conventional seed sorting techniques may require asample of seeds to be re-evaluated through multiple seed sorting passes.

Some processes have been disclosed for visualizing green fluorescentprotein (GFP) expression in transgenic plants in order to selecttransgenic seeds as described, for example, in U.S. Pat. No. 6,947,144to Kim et al. In particular, the Kim reference describes a system forseparating seeds transformed with a green fluorescent protein (GFP) thatincludes a light source 5′ filtered through a band pass filter 6′. Thelight source 5′ is positioned above and at a 45° angle from plantsamples traveling on a conveyor belt 3′. A CCD camera 9′ is alsopositioned above the conveyor belt 3′, directly above the examined plantsample 4′. The CCD camera 9′ detects light generated from a portion ofthe surface area of the plant sample through a filter 7′. See, e.g., theKim reference, FIG. 9.

However, the system disclosed by the Kim reference suffers from severalinsufficiencies. For example, there are a number of different traits,including the expression of fluorescent proteins, for which the accuratemeasurement of a seed in more than a portion of the surface area of theseed may be important. In some instances, the expression of afluorescent protein may not be uniform across entire surface area of aseed. Thus, if a localized area of the seed expresses the fluorescentprotein and that area is facing downward (such as against the conveyorbelt in the Kim reference) the CCD camera will not detect thefluorescent protein and the seed will not be correctly sorted.

In addition, the use of GFP for identification and/or selection oftransgenic plant material presents several technical challenges. Firstof all, the excitation and emission wavelengths for GFP visualizationare on the fringes of the visible spectrum, and are therefore not easilyvisible to the eye (or to many conventional visualization systems) usingnormal “white” light that is present in conventional research and/ormanufacturing environments. Furthermore, it has been noted that GFP mayresult in protein aggregation in vivo in plant material that has beentagged with GFP. It is well-known that unchecked protein aggregation maynot only produce adverse effects in seed product, but may also produceunwanted environmental effects if GFP-tagged seeds are introduced intoan agricultural environment that interacts with external ecologicalsystems (such as forests and/or wetlands adjacent to an agriculturalresearch plot).

As a result, there is a need for a method and computer program productfor distinguishing seeds that contain a marker associated with aselected genotype from a bulk sample of seeds. The method and computerprogram product should permit a bulk sample to be sorted based on thepresence of the marker or the absence of the marker, and should providea level of convenience, accuracy, speed and environmental safety that isnot available using conventional techniques. In some embodiments, themethod should provide for improved accuracy in seed sorting, thussubstantially avoiding the need for multiple seed sorting passes.Additionally, in some embodiments the method and computer programproduct should provide the ability to accurately sort a bulk sample ofseeds based on the presence or absence of markers associated with aselected genotype using commercially-available high-speed sortingequipment with minimal modifications.

BRIEF SUMMARY OF VARIOUS EMBODIMENTS

The embodiments of the present invention satisfy the needs listed aboveand provide other advantages as described below. Some embodiments of thepresent invention may include a method for distinguishing seedscontaining a genetic element of interest from a bulk sample byassociating a discernable marker with at least some of the seedscontaining a genetic element of interest of the bulk sample, evaluatingat least some of the seeds of the bulk sample for the presence orabsence of the marker using an evaluating device, and sorting the seedscontaining a genetic element of interest based on the presence orabsence of the marker.

In some embodiments the seeds are excited using an photonic emittingdevice configured to excite a majority of the surface area of the seeds.In some embodiments, exciting the seeds using a photonic emitting devicecomprises exciting the seeds using at least one illuminating deviceconfigured to illuminate a majority of the surface area of the seeds. Insome embodiments, exciting the seeds using at least one illuminatingdevice further comprises using two or more illuminating devices arrangedto collectively illuminate a majority of the surface area of the seeds.In some embodiments, evaluating at least some of the seeds of the bulkcomprises evaluating at least some of the seeds of the bulk sample usingat least one image sensing device arranged to receive emissions from amajority of the surface area of the seeds. In some embodiments,evaluating at least some of the seeds of the bulk sample furthercomprises using two or more image sensing devices arranged tocollectively receive emissions from a majority of the surface area ofthe seeds.

Other embodiments of the present invention may include a method andcomputer program product for distinguishing seeds containing a geneticelement of interest from a bulk sample by associating a discernable redfluorescent protein (RFP) marker with at least some of the seedscontaining a genetic element of interest of the bulk sample, evaluatingat least some of the seeds of the bulk sample for the presence orabsence of the RFP marker using an evaluating device, and sorting theseeds containing a genetic element of interest based on the presence orabsence of the RFP marker.

In some embodiments, the RFP marker is discernable when excited by acertain energy having a wavelength ranging from substantially about 500nm to substantially about 580 nm. In some such embodiments, the certainenergy may have a peak at substantially about 550 nm. In otherembodiments, the evaluating step comprises exciting the seeds containinga genetic element of interest with the certain energy; and detecting anemission resulting at least in part from the exciting step. In some suchembodiments, the resulting emission may have a wavelength ranging fromsubstantially about 500 nm to substantially about 600 nm. Furthermore,the emission may have a peak at substantially about 580 nm. In someembodiments, the evaluating device may further comprise at least onefilter disposed substantially between the image sensing device and theseeds containing a genetic element of interest. The filter may beconfigured for passing the emission from the red fluorescent proteinmarker to the image sensing device.

Some embodiments may further comprise associating a plurality ofsupplemental markers with at least some of the seeds containing acorresponding plurality of additional genetic elements of interest ofthe bulk sample. Such embodiments may further comprise steps forevaluating at least one of the seeds of the bulk sample for the presenceor absence of the plurality of supplemental markers using the evaluatingdevice, and sorting the seeds containing the plurality of additionalgenetic elements of interest based on the presence or absence of the aplurality of supplemental markers. In such embodiments, the supplementalmarkers may include, but are not limited to: yellow fluorescentproteins; yellow/orange fluorescent proteins; orange fluorescentproteins; orange/red fluorescent proteins; red/orange fluorescentproteins; red fluorescent proteins; cyan fluorescent proteins; andcombinations of such supplemental markers.

In some embodiments, the evaluating device may be a seed color sorter.In other embodiments, the image sensing device may be a charge-coupleddevice (CCD device) or a complementary metal oxide semiconductor (CMOS)device. In other embodiments, the evaluating step comprises evaluatingseeds for the presence of a RFP marker using at least one image sensingdevice configured to differentiate between a range of normal seedemissions and the discernable RFP marker. In other embodiments, thesorting step may comprise dispensing the sorted individual seeds into atleast one container, the container including only seeds having the RFPmarker present or only seeds in which the RFP marker is absent.

Other embodiments further comprise steps for singulating individualseeds from the bulk sample using a singulating device. In someembodiments, the singulating step comprises singulating seeds using aplurality of elongate hollow structures operatively connected to avacuum source. In other embodiments, the singulating step comprisesreceiving the bulk sample in a hopper and vibrating the hopper so as topropel individual seeds along an inclined spiral ramp and through a gapconfigured to permit the passage of one seed at a time. In otherembodiments, the singulating step comprises receiving the bulk sample ina hopper, feeding seeds from the hopper to a rotatable disk, androtating the rotatable disk so as to distribute the seeds to a peripheryof the rotatable disk by application of centrifugal force. In otherembodiments, the singulating step comprises receiving the bulk sample ina hopper, vibrating the bulk sample such that seeds tend to move towardsan opening in the hopper, distributing seeds from the opening in thehopper to a sloped device that includes at least one groove such that aline of individual seeds is formed in the groove, and depositingindividual seeds by gravity force from the sloped device onto aconveying device.

Another embodiment provides a method that comprises associating afluorescent protein marker with at least some of the seeds containing agenetic element of interest, placing a portion of the seeds from thebulk sample within an open-faced enclosure configured for use as aportable table-top evaluating device, exciting at least some of theportion of seeds with a light source, manually inspecting the excitedseeds, and manually sorting the excited seeds based on the presence orabsence of the protein marker. In some embodiments, manually inspectingthe excited seeds may comprise manually inspecting the excited seeds byviewing the excited seeds through a filter of the enclosure. In someembodiments, manually inspecting the excited seeds may comprise manuallyinspecting the excited seeds by viewing the excited seeds through amagnifying lens. In some embodiments, associating a fluorescent proteinmarker with at least some of the seeds containing a genetic element ofinterest may comprise associating a red fluorescent protein marker withat least some of the seeds containing a genetic element of interest, andmanually inspecting the excited seeds may comprise manually inspectingthe excited seeds by viewing the excited seeds through a red band passfilter of the enclosure. In some embodiments, manually inspecting theexcited seeds may comprise manually inspecting the excited seeds byviewing the excited seeds through filtered eyewear. In some embodiments,manually inspecting the excited seeds may comprise manually inspectingthe excited seeds by viewing the excited seeds through red band passfiltered eyewear. In some embodiments, exciting at least some of theportion of seeds with a light source may comprise exciting at least someof the portion of seeds with an LED light source. In some embodiments,exciting at least some of the portion of seeds with an LED light sourcemay comprise exciting at least some of the portion of seeds with an LEDarray light source. In some embodiments, exciting at least some of theportion of seeds with a LED light source may comprise exciting at leastsome of the portion of seeds with a green LED light source. In someembodiments, exciting at least some of the portion of seeds with an LEDlight source may comprise exciting at least some of the portion of seedswith a green LED array light source.

Another embodiment provides a method that comprises associating a redfluorescent protein marker with at least some of the seeds containing agenetic element of interest, loading a portion of the seeds from thebulk sample into a hopper and feeding the portion of seeds onto a traydefining a tray length, automatically moving the portion of seeds alongthe tray length, exciting at least some of the portion of seeds on thetray with an LED light source, manually inspecting the excited seeds,and manually sorting the seeds based on the presence or absence of thered fluorescent protein marker. In some embodiments, manually inspectingthe excited seeds may comprise manually inspecting the excited seeds byviewing the excited seeds through a filter. In some embodiments,manually inspecting the excited seeds may comprise manually inspectingthe excited seeds by viewing the excited seeds through a magnifyinglens. In some embodiments, manually inspecting the excited seeds maycomprise manually inspecting the excited seeds by viewing the excitedseeds through a red band pass filter. In some embodiments, exciting atleast some of the portion of seeds with an LED light source may compriseexciting at least some of the portion of seeds with an LED array. Insome embodiments, exciting at least some of the portion of seeds with anLED light source may comprise exciting at least some of the portion ofseeds with a green LED light source. In some embodiments, exciting atleast some of the portion of seeds with an LED light source may compriseexciting at least some of the portion of seeds with a green LED arraylight source. In some embodiments, automatically moving the portion ofseeds along the tray length may comprise vibrating the tray with avibration generating device. In some embodiments, manually inspectingthe excited seeds may comprise manually inspecting the excited seeds byviewing the excited seeds through filtered eyewear. In some embodiments,manually inspecting the excited seeds may comprise manually inspectingthe excited seeds by viewing the excited seeds through red band passfiltered eyewear.

Another embodiment provides a method that comprises associating a redfluorescent protein marker with at least some of the seeds containing agenetic element of interest, loading a portion of the seeds from thebulk sample into a hopper, exciting at least some of the portion ofseeds with an LED light source; automatically feeding the portion ofseeds past an image sensing device, and automatically sorting theexcited seeds based on the presence or absence of the red fluorescentprotein marker. In some embodiments, exciting at least some of theportion of seeds with an LED light source may comprise exciting at leastsome of the portion of seeds with an LED array. In some embodiments,exciting at least some of the portion of seeds with an LED light sourcemay comprise exciting at least some of the portion of seeds with a greenLED light source. In some embodiments, exciting at least some of theportion of seeds with an LED light source may comprise exciting at leastsome of the portion of seeds with a green LED array light source.

Thus the various embodiments of distinguishing seeds containing agenetic element of interest of the present invention provide manyadvantages that may include, but are not limited to: providing a methodand computer program product capable of permitting a bulk sample ofseeds to be sorted based on the presence or absence of a marker ormultiple RFP markers, associated with a selected genotype, or multipleselected genotypes. The present invention provides a level ofconvenience, speed, accuracy, and environmental safety that is notavailable using conventional techniques. Additionally, the presentinvention provides additional processing of the sorted seeds, includingdispensing the sorted seeds into containers.

These advantages, and others that will be evident to those skilled inthe art, are provided in the method and computer program product of thepresent invention.

BRIEF DESCRIPTION OF THE DRAWINGS

Having thus described the invention in general terms, reference will nowbe made to the accompanying drawings, which are not necessarily drawn toscale, and wherein:

FIG. 1 shows a flow chart of a method, according to one embodiment ofthe present invention, including steps for associating a marker withseeds containing a genetic element of interest, evaluating the seeds forthe presence of the marker, and sorting the seeds based on the presenceor absence of the marker;

FIG. 2 shows a non-limiting schematic of a seed sorter device used todistinguish seeds containing a genetic element of interest in accordancewith one embodiment of the present invention;

FIG. 3 shows a non-limiting schematic of a system incorporating a vacuumdrum singulating device for singulating seeds prior to evaluating andseparating seeds based on the presence of a marker in accordance withone embodiment of the present invention;

FIG. 4 shows a non-limiting schematic of a system incorporating a hopperhaving an inclined ramp for singulating seeds prior to evaluating andseparating seeds based on the presence of a marker in accordance withone embodiment of the present invention;

FIG. 5 shows a non-limiting schematic of a system incorporating arotatable disk for singulating seeds prior to evaluating and separatingseeds based on the presence of a marker in accordance with oneembodiment of the present invention; and

FIG. 6 shows a non-limiting schematic of a system incorporating aninclined ramp having a groove feature for singulating seeds prior toevaluating and separating seeds based on the presence of a marker inaccordance with one embodiment of the present invention;

FIG. 7 shows a non-limiting block diagram of an exemplary electronicdevice configured to distinguish genetically transferred seeds from abulk sample of exemplary embodiments of the present invention;

FIG. 8 shows a non-limiting schematic of a seed sorter device used todistinguish seeds containing a genetic element of interest in accordancewith one embodiment of the present invention;

FIG. 9 shows a non-limiting schematic of a system incorporating a vacuumdrum singulating device and a pair of illuminating devices in accordancewith one embodiment of the present invention;

FIG. 10 shows a non-limiting schematic of a seed sorter deviceincorporating a pair of illuminating devices and a pair of evaluatingdevices used to distinguish seeds containing a genetic element ofinterest in accordance with one embodiment of the present invention;

FIG. 11 shows a non-limiting perspective view of a portable evaluatingdevice in accordance with another embodiment of the present invention;

FIG. 12 shows non-limiting perspective view of another system forevaluating and sorting seeds in accordance with another embodiment ofthe present invention; and

FIG. 13 shows a non-limiting schematic of another device for evaluatingand sorting seeds in accordance with an additional embodiment of thepresent invention.

DETAILED DESCRIPTION

The present invention now will be described more fully hereinafter withreference to the accompanying drawings, in which some, but not allembodiments of the invention are shown. Indeed, this invention may beembodied in many different forms and should not be construed as limitedto the embodiments set forth herein; rather, these embodiments areprovided so that this disclosure will satisfy applicable legalrequirements. Like numbers refer to like elements throughout.

Under current methods, it is difficult to distinguish, prior togermination, seeds that contain a genetic element of interest from seedsthat do not contain such elements. To address this concern, variousembodiments of the present invention provide a method and computerprogram product that sorts seeds based at least in part on therelationship between a discernable marker and one or more seedscontaining a genetic element of interest. For the purposes of thecurrent specification and the appended claims, the term “discernable”refers to an ability to recognize a marker when excited by certainenergy. In various embodiments, this may include the visible portion ofthe photonic spectrum, as well as Ultraviolet and Infrared spectrums.

FIG. 1 shows a flowchart illustrating a method 10 for distinguishingseeds containing a genetic element of interest from a bulk sample. Instep 12, a marker is associated with at least a portion of seedscontaining a genetic element of interest from the bulk sample. Invarious embodiments, associating a marker with at least a portion ofseeds containing a genetic element of interest may comprise a variety oftechniques used to mark a desired genotype. In an exemplary embodiment,associating a marker with at least a portion of seeds containing agenetic element of interest comprises attaching DNA sequences that codefor red fluorescent protein (RFP) to a desired trait DNA sequence thatis inserted into a seed or a group of seeds. It should be noted thatalthough the exemplary embodiment described below associates an RFPmarker with a desired trait, in other embodiments multiple fluorescentprotein (FP) markers may be associated with a desired trait DNA sequenceor multiple desired trait DNA sequences in the same seed. Suchadditional FP markers may include, but are not limited to: yellow;yellow/orange; orange; orange/red, red/orange; red (including the RFPdescribed herein); and cyan. In other embodiments, the marker maycomprise phenotypic markers such as β-galactosidase and fluorescentproteins such as cyan florescent protein (CYP) (Bolte et al. (2004) J.Cell Science 117:943-54 and Kato et al. (2002) Plant Physiol129:913-42), and yellow florescent protein (PhiYFP™ from Evrogen, see,Bolte et al. (2004) J. Cell Science 117:943-54). For additionalselectable markers, see generally, Yarranton (1992) Curr. Opin. Biotech.3:506-511; Christopherson et al. (1992) Proc. Natl. Acad. Sci. USA89:6314-6318; Yao et al. (1992) Cell 71:63-72; Reznikoff (1992) Mol.Microbiol. 6:2419-2422; Barkley et al. (1980) in The Operon, pp.177-220; Hu et al. (1987) Cell 48:555-566; Brown et al. (1987) Cell49:603-612; Figge et al. (1988) Cell 52:713-722; Deuschle et al. (1989)Proc. Natl. Acad. Aci. USA 86:5400-5404; Fuerst et al. (1989) Proc.Natl. Acad. Sci. USA 86:2549-2553; Deuschle et al. (1990) Science248:480-483; Gossen (1993) Ph.D. Thesis, University of Heidelberg;Reines et al. (1993) Proc. Natl. Acad. Sci. USA 90:1917-1921; Labow etal. (1990) Mol. Cell. Biol. 10:3343-3356; Zambretti et al. (1992) Proc.Natl. Acad. Sci. USA 89:3952-3956; Bairn et al. (1991) Proc. Natl. Acad.Sci. USA 88:5072-5076; Wyborski et al. (1991) Nucleic Acids Res.19:4647-4653; Hillenand-Wissman (1989) Topics Mol. Struc. Biol.10:143-162; Degenkolb et al. (1991) Antimicrob. Agents Chemother.35:1591-1595; Kleinschnidt et al. (1988) Biochemistry 27:1094-1104;Bonin (1993) Ph.D. Thesis, University of Heidelberg; Gossen et al.(1992) Proc. Natl. Acad. Sci. USA 89:5547-5551; Oliva et al. (1992)Antimicrob. Agents Chemother. 36:913-919; Hlavka et al. (1985) Handbookof Experimental Pharmacology, Vol. 78 (Springer-Verlag, Berlin); Gill etal. (1988) Nature 334:721-724. Such disclosures are herein incorporatedby reference. In other embodiments, the marker may also comprise aselectable marker gene for the selection of transformed cells.

The above lists are not meant to be limiting. Any desired trait andmarker may be used in the present invention.

In various embodiments, the desired trait DNA sequence may correspondsubstantially to any trait desired to be inserted into a plant genome.

In one exemplary embodiment, the marker associated with at least aportion of seeds containing a genetic element of interest from the bulksample in step 12 may comprise a RFP marker such as the DsRed and/orDsRed2 RFP markers from the Living Colors™ line of novel fluorescentproteins (NFP) commercially available from Clontech Laboratories, Inc.of Mountain View, Calif. The use of RFP as the marker may provideseveral advantages over other fluorescent protein markers (such as greenfluorescent protein (GFP)). For example, unlike GFP, RFP excitation andemission wavelengths are closer to a center of the visible range of thephotonic spectrum. Therefore, RFP-expressing seed may be visible to theeye (and unassisted and/or unmodified cameras or other sensor devices)in ‘normal’ ambient white light. Thus, seed sorting (step 16, forexample) may be accomplished in such embodiments without the need forspecialized UV light sources and/or detectors. Furthermore, manycommercially available and industry-proven high-speed sorting devicesoperate most effectively in the visible range of the photonic spectrum.Again as above, since RFP excitation and emission wavelengths arepredominantly centered in the visible range of the photonic spectrum,sorting (step 16) may be accomplished using existing andreadily-available equipment as an add-on to the current use for morestandard quality sorting procedures. Furthermore, RFP (and specificallyDsRed2) markers are optimized for minimal protein aggregation, such thatthe marker may avoid issues with in vivo protein aggregation that mayaffect product performance (i.e. seed viability and/or yield) as well asproduce potentially negative environmental effects that run counter toprinciples of product stewardship.

Step 12 may comprise, in some embodiments, associating the RFP markerwith one or more desired trait DNA sequences that may be inserted into aseed or a group of seeds. For example, genetically engineered plantsand/or seeds may contain beneficial traits of interest such as one ormore genes expressing peptides with pesticidal and/or insecticidalactivity, such as Bt toxic proteins (described in, for example, U.S.Pat. Nos. 5,277,905; 5,366,892; 5,747,450; 5,723,756; 5,859,336;5,593,881; 5,625,136; 5,689,052; 5,691,308; 5,188,960; 6,180,774;6,023,013; 6,218,188; 6,342,660; 6,114,608; and 7,030,295; USPublication Nos: US20040199939 and US20060085870; WO2004086868; andGeiser et al. (1986) Gene 48:109) and Bt crystal proteins of the Cry34and Cry35 classes (see, e.g., Schnepf et al. (2005) Appl. Environ.Microbiol. 71:1765-1774), and vegetative insecticidal proteins (forexample, members of the VIP1, VIP2, or VIP3 classes, see, for example,U.S. Pat. Nos. 5,849,870; 5,877,012; 5,889,174; 5,990,383; 6,107,279;6,137,033; 6,291,156; 6,429,360; as well as US Pat. App. PublicationNos: US20050210545; US20040133942; and US20020078473), lectins (VanDamme et al. (1994) Plant Mol. Biol. 24:825, pentin (described in U.S.Pat. No. 5,981,722), lipases (lipid acyl hydrolases, see, e.g., thosedisclosed in U.S. Pat. Nos. 6,657,046 and 5,743,477), cholesteroloxidases from Streptomyces, and pesticidal proteins derived fromXenorhabdus and Photorhabdus bacteria species, Bacillus laterosporusspecies, and Bacillus sphaericus species, and the like. Alsocontemplated is the use of chimeric (hybrid) toxins (see, e.g., Bosch etal. (1994) Bio/Technology 12:915-918).

Genetically engineered plants and/or seeds thereof can also contain oneor more genes with a variety of desired trait combinations including,but not limited to, traits desirable for animal feed such as high oilgenes (e.g., U.S. Pat. No. 6,232,529); balanced amino acids (e.g.,hordothionins (U.S. Pat. Nos. 5,990,389; 5,885,801; 5,885,802; and5,703,049); barley high lysine (Williamson et al. (1987) Eur. J.Biochem. 165:99-106; and WO 98/20122) and high methionine proteins(Pedersen et al. (1986) J. Biol. Chem. 261:6279; Kirihara et al. (1988)Gene 71:359; and Musumura et al. (1989) Plant Mol. Biol. 12:123));increased digestibility (e.g., modified storage proteins (U.S. Pat. No.6,858,778); and thioredoxins (U.S. Pat. No. 7,009,087)). Such plants canalso contain one or more genes resulting in traits desirable for diseaseresistance (e.g., fumonisin detoxification genes (U.S. Pat. No.5,792,931); avirulence and disease resistance genes (Jones et al. (1994)Science 266:789; Martin et al. (1993) Science 262:1432; Mindrinos et al.(1994) Cell 78:1089).

Genetically modified plants may further contain one or more genesencoding one or more forms of herbicide resistance, for example, toglyphosate-N-(phosphonomethyl)glycine (including the isopropylamine saltform of such herbicide). Exemplary herbicide resistance genes includeglyphosate N-acetyltransferase (GAT) and5-enolpyruvylshikimate-3-phosphate synthase (EPSPS), including thosedisclosed in US Pat. Application Publication Nos: US20040082770, alsoWO02/36782 and WO03/092360). Herbicide resistance genes generally codefor a modified target protein insensitive to the herbicide or for anenzyme that degrades or detoxifies the herbicide in the plant before itcan act. See, e.g., DeBlock et al. (1987) EMBO J. 6:2513; DeBlock et al.(1989) Plant Physiol. 91:691; Fromm et al. (1990) BioTechnology 8:833;Gordon-Kamm et al. (1990) Plant Cell 2:603; and Frisch et al. (1995)Plant Mol. Biol. 27:405-9. For example, resistance to glyphosate orsulfonylurea herbicides has been obtained using genes coding for themutant target enzymes, EPSPS and acetolactate synthase (ALS). Resistanceto glufosinate ammonium, bromoxynil, and 2,4-dichlorophenoxyacetate(2,4-D) have been obtained by using bacterial genes encodingphosphinothricin acetyltransferase, a nitrilase, or a2,4-dichlorophenoxyacetate monooxygenase, which detoxify the respectiveherbicides. Also contemplated are inhibitors of glutamine synthase suchas phosphinothricin or basta (e.g., bar gene).

Transgenic plants and/or seeds may also contain one or more genesresulting in traits desirable for processing or process products such asmodified oils (e.g., fatty acid desaturase genes (U.S. Pat. Nos.5,952,544; 6,372,965)); modified starches (e.g., ADPG pyrophosphorylases(AGPase), starch synthases (SS), starch branching enzymes (SBE), andstarch debranching enzymes (SDBE)); and polymers or bioplastics (e.g.,U.S. Pat. No. 5,602,321; beta-ketothiolase, polyhydroxybutyratesynthase, and acetoacetyl-CoA reductase (Schubert et al. (1988) J.Bacteriol. 170:5837-5847)). Such plants could also contain one or moregenes providing agronomic traits such as male sterility (e.g., see U.S.Pat. No. 5,583,210), stalk strength, flowering time, or transformationtechnology traits such as cell cycle regulation or gene targeting (e.g.,WO 99/61619, U.S. Pat. Nos. 6,518,487 and 6,187,994).

In step 14, the seeds from the bulk sample are evaluated for thepresence or absence of the RFP marker. In various embodiments, this step14 may comprise visually determining whether the RFP marker is presentor absent in a seed or a group of seeds. In an exemplary embodiment,step 14 comprises exciting seeds from the bulk sample with a certainenergy and then determining whether the RFP marker is present. Thecertain energy used to illuminate the seeds (and/or excite the RFPmarkers that may be present therein) may have a wavelength substantiallywithin the visible photonic spectrum (i.e. a wavelength ranging fromsubstantially about 500 nm to substantially about 580 nm). In someembodiments the certain energy emitted as part of step 14 may exhibit apeak at substantially about 550 nm. In some embodiments, step 14 mayfurther comprise detecting an emission resulting at least in part fromthe exciting step, wherein the emission may have a wavelength rangingfrom substantially about 500 nm to substantially about 600 nm. In someembodiments, the emission resulting from step 14 may exhibit a peak atsubstantially about 580 nm.

Various evaluating devices may be used for the determination performedin step 14. For example, evaluating devices may include, but are notlimited to, commercially available optical seed sorters, such as aScanMaster II seed sorter manufactured by Satake-USA. Although in normalusage, seed sorters may be used to evaluate and sort out contaminantssuch as rocks, glass, soil, damaged food items, mold, and other foreignmaterial from a bulk sample of food items, an exemplary embodiment ofthe present invention modifies a seed sorter to evaluate and sort seedsexpressing a fluorescent protein that is attached to a desired trait DNAsequence that has been inserted into a seed or a group of seeds in thebulk sample.

As shown generally in FIG. 8, such optical seed sorters may include aspecialized vision system 54 which, in some embodiments, may comprise:(1) an illuminating device 54 a (such as a bulb, for example) that emitslight at a particular wavelength (characterizing the “certain energy”described herein) chosen to illuminate and thereby “excite” the RFPmarker, and (2) a filter 54 b used that may be used to filter the energyemitted (i.e. “the emission”) from the RFP-tagged seeds so that a camera54 c (or other image sensing device) of the vision system may discernseeds expressing the RFP marker.

To accomplish this task, in one method embodiment of the presentinvention, the evaluating step 14 may comprise evaluating seeds for thepresence of the RFP marker using at least one image sensing device 54 cconfigured to differentiate between a range of normal seed emissions andan emission from the RFP marker. As described herein, such an imagesensing device 54 c may comprise a component of a commercially availablecolor sorter device. Furthermore, in some embodiments, the image sensingdevice 54 c may comprise a CCD device and/or a CMOS device configuredfor detecting the emission from RFP-tagged transgenic and/or otherwisegenetically-modified seeds.

As shown in FIG. 8, in some embodiments, the evaluating device employedas part of the evaluating step 14 may further comprise at least onefilter 54 b disposed substantially between an image sensing device 54 c(such as a CCD) and the seeds containing a genetic element of interest.The at least one filter 54 b may be configured for passing the emissionfrom the red fluorescent protein marker to the image sensing device 54c. For example, in some embodiments, the filter 54 b may comprise a bandpass filter configured for passing light having a wavelength that issubstantially equivalent to the targeted emission wavelength (i.e. theemission wavelength of energy emitted from an illuminated andsubsequently excited RFP marker (such as DsRed2, for example). Theemission may then be detected by the image sensing device 54 c that maybe further configured for translating the emission into substantially“white” light. Thus, the image sensing device may assign substantiallybinary values to each seed based on the presence or absence of the RFPmarker wherein seeds containing a genetic element of interest (taggedwith the relatively “bright” RFP marker) are marked “positive” (andthereby deflected and/or other wise directed into one or more “+”containers 56. Seeds that do not contain a genetic element of interest,or other particulate debris (which may be translated into a “dark” or“negative” result) may be dropped and/or otherwise directed into one ormore “−” containers 58. As shown in FIG. 8, the image sensing device 54c (or other component of a vision system 54 may be in communication witha sorting device 55 (which may comprise, for example, a valve deviceand/or compressed air jet device) configured for directing the“positive” (i.e. seeds containing a genetic element of interest (whichthe image sensing device 54 c may detect as “white” or “bright” seeds))into one or more “+” containers 56 in response to a binary positive or“1” signal received from the image sensing device 54 c or otherprocessing component of the vision system 54. The sorting device 55 mayalso be configured for directing the “negative” (i.e. seeds that do notcontain a genetic element of interest or particulate debris (which theimage sensing device 54 c may detect as “dark” seeds)) into one or more“−” containers 58 in response to a binary negative or “0” signalreceived from the image sensing device 54 c or other processingcomponent of the vision system 54. While the system 50 shown in FIG. 8is shown oriented in a substantially vertical orientation (such thatindividual seeds pass through the vision system components 54 a, 54 b,54 c in response to gravity forces) in should be understood that thesystem 50 may also be oriented substantially horizontally and maycomprise one or more pressurized pneumatic tubes and/or conveyancepathways configured for directing individual seeds from a sample pastthe various vision system components 54 a, 54 b, 54 c and subsequentlyto a sorting device 55 that may be configured for transferring the seedscontaining a genetic element of interest into corresponding “+”containers 56 and for transferring the seeds not containing the geneticelement of interest into corresponding “−” containers 58 in response tosignals received from one or more vision system 54 components and/orcontrollers.

As described herein, some embodiments of the present invention mayutilize a plurality of supplemental markers (such as a variety offluorescent protein markers) to highlight the presence and/or absence ofa corresponding plurality of additional genetic elements of interest inthe seeds of the bulk sample. For example, as described herein, variousembodiments of the present invention may utilize supplemental markersthat may include, but are not limited to: yellow fluorescent proteins;yellow/orange fluorescent proteins; orange fluorescent proteins;orange/red fluorescent proteins; red/orange fluorescent proteins; redfluorescent proteins; cyan fluorescent proteins; and combinations ofsuch supplemental markers. Referring generally to FIG. 1, suchembodiments may comprise step 12 for associating one or more of aplurality of supplemental markers with at least some of the seedscontaining a corresponding plurality of additional genetic elements ofinterest of the bulk sample. Some such embodiments may further comprisestep 14 for evaluating at least one of the seeds of the bulk sample forthe presence or absence of the plurality of supplemental markers usingthe evaluating device and subsequently, step 16 for sorting the seedscontaining the plurality of additional genetic elements of interestbased on the presence or absence of the a plurality of supplementalmarkers.

In some such embodiments, the evaluating step 14 may comprise evaluatingseeds for the presence of at least one of the plurality of supplementalmarkers using at least one image sensing device 54 configured todifferentiate between a range of normal seed emissions and at least oneemission from one or more of the plurality of supplemental markers. Asdescribed herein, in some embodiments, the image sensing device 54 maycomprise a CCD device or a CMOS device. As shown generally in FIG. 8,the evaluating device used to perform the evaluating step 14 maycomprise a specialized vision system 54 which, in some embodiments, maycomprise: (1) an illuminating device 54 a (such as a bulb, for example)that emits light at a particular wavelength (characterizing the “certainenergy” described herein) chosen to illuminate and thereby “excite” theRFP marker, and (2) a filter 54 b used that may be used to filter theenergy emitted (i.e. “the emission”) from the RFP-tagged seeds so that acamera 54 c (or other image sensing device) of the vision system maydiscern seeds expressing the RFP marker. In some embodiments wherein aplurality of supplemental markers (which may each exhibit acharacteristic emission wavelength, for example) are used to “tag” acorresponding plurality of additional genetic elements that may bepresent in the seeds, the filter 54 b may comprise at least one tunablefilter disposed substantially between the image sensing device 54 c andthe seeds containing a genetic element of interest. The at least onetunable filter 54 b may be configured for selectively passing the atleast one emission from one or more of the plurality of supplementalmarkers to the image sensing device 54 c. In such embodiments, thetunable filter 54 c may allow the evaluating device to selectively sortfor a plurality of different genetic elements of interest that may bepresent in the seed sample. In one exemplary embodiment, the filterdevice 54 c may comprise a VariSpec™ Liquid Crystal Tunable Filter(LCTF) commercially available from CRI, Inc. of Woburn, Mass. In somesuch embodiments, the filter 54 b may be “tuned” to sequentially senseand sort seeds based on “positive” emissions from seeds having oneparticular genetic element of interest (that corresponds, for example,to one of a plurality of supplemental markers and/or the base RFP)during a sequence of passes through the evaluating device 54.

FIG. 2 shows a schematic representation of another exemplary system 50that may be used to distinguish seeds containing a genetic element ofinterest from a bulk sample of seeds in accordance with one exemplaryembodiment. In the exemplary embodiment, the system 50 is a modifiedcommercially available seed sorter. A bulk sample A of seeds, at leastsome of which have been genetically transformed by inserting a desiredtrait DNA sequence with an attached DNA sequence that codes forfluorescent proteins, are loaded into a hopper 52. The hopper 52 isconfigured to funnel the bulk sample A of seeds into separate chutes 53that are sized to accommodate a particular volume for processing by avision system 54. The seeds from each chute 53 fall by force of gravitypast the vision system 54. In the exemplary embodiment, the visionsystem 54 comprises an illuminating device, at least one sensing device,and a controller configured to control the illuminating and sensingdevices.

In the exemplary embodiment, the illuminating device comprises a lightsource that uses a bulb configured to emit light at a wavelengthspectrum that illuminates the RFP marker. In other embodiments, thelight source may be any light source that permits the image sensingdevice to discern the RFP marker. As such, in various embodiments thelight source and the marker may be paired so as to increase the abilityof the vision system to discern the presence of the marker. Theexemplary embodiment includes multiple CCD cameras with filters (i.e.red band pass filters) configured to enhance the illumination and to aidin discerning the presence of the RFP marker. Although other embodimentsmay use fewer cameras, the exemplary embodiment allows seeds fallingpast the vision system 54 to be viewed from the front and back. In otherembodiments, any vision system 54 configured to discern the presence ofa RFP marker may be used, including, but not limited to, CCD devices,CMOS devices and other vision sensors.

Step 16 of FIG. 1 relates to sorting the seeds containing a geneticelement of interest based on the presence or absence of the marker. Thesorting function is carried out by a sorting device. In the exemplaryembodiment shown in FIG. 2, the sorting device 55 comprises a number ofindividual pneumatic ejectors that emit a controlled blast of air (suchas an “air knife” for example) configured for sorting seeds that exhibitthe RFP marker as the seeds pass through the sorting device. Seedsexhibiting the RFP marker are sorted into containers 56, identified inthe figure with a “+” symbol. Seeds that do not contain the marker fallinto containers 58, identified in the figure with a “−” symbol. Althoughnot shown in the figure, in other embodiments the seeds contained in the“−” container 58 may be re-routed through the hopper 52 so that theseseeds make a successive pass through the system 50. In such a manner anyseeds that were not identified as exhibiting the marker may beidentified in one or more successive passes through the system 50.

The above described method allows the processing of a large quantity ofseeds, a portion of which include a marker that is associated with agenetically transformed seed including a desired trait. However in otherembodiments, a bulk sample may include various seeds having differentmarkers associated with different desired traits, or seeds that includemore than one marker associated with different desired traits. Althoughthe exemplary embodiment described above may accommodate thesesituations, in other instances it may be advantageous to evaluate seedson a seed-by-seed basis. As a result, in various embodiments, thepresent invention contemplates singulating seeds from a bulk sampleprior to evaluating the seeds for the presence or absence of a marker ora group of markers associated with a desired trait or group of traits.

FIG. 3 shows a system 100 employing the above method in accordance withone embodiment of the present invention. The system 100 shown in thefigure includes an exemplary embodiment of a singulating devicecomprising a plurality of elongate hollow structures operativelyconnected to a vacuum source used to singulate seeds from a bulk sample.Specifically, the system 100 of the exemplary embodiment includes ahopper 102 into which a bulk sample A of seeds may be placed. A rotatingdrum 104 is positioned adjacent the hopper 102. The rotating drum 104includes a plurality of elongate hollow structures 106 that extend intoa substantially hollow interior of the drum 104, which is connected to avacuum source (not shown). The vacuum source creates a zone of negativepressure within the interior of the drum 104, and as a result, distalends of the elongate hollow structures 106 create discrete areas ofnegative pressure. As shown in the figure, the drum 104 rotates adjacentan open end of the hopper 102. The hopper 102 is configured such thatseeds are urged toward the open end and adjacent the rotating drum 104.The drum 104 rotates in the direction shown such that the elongatehollow structures 106 pass through a portion of the seeds of the bulksample A adjacent the drum 104. As the elongate hollow structures 106rotate through the bulk sample A, the discrete areas of negativepressure located at the distal ends of the elongate hollow structures106 attract individual seeds 101. The size of the distal ends of each ofthe elongate hollow structures 106 is configured such the discrete areaof negative pressure at the distal end of each of the hollow structures106 attracts a single seed 101. As shown in the figure, as the elongatehollow structures 106 rotate through the open end of the hopper 102,individual seeds 101 attach to the distal ends of the elongate hollowstructures 106. As the drum 104 continues to rotate in the directionshown, the seeds 101 travel toward a conveyor belt 110. Rotating drivingmembers 112 drive the conveyor belt 110 in the direction shown. Invarious embodiments, the speed of the driving members 112 may beadjusted to optimize downstream evaluating and sorting of the seeds 101.

At a position adjacent the conveyor belt 110, a deflector plate 108 (oralternatively, in some embodiments, a compressed air source configuredfor detaching individual seeds from the elongate hollow structures 106)deflects the seeds 101 from the distal ends of the elongate hollowstructures 106 and onto the conveyor belt 110. In the exemplaryembodiment, the deflector plate 108 contacts between the distal ends ofthe elongate hollow structures 106 and the seeds 101 carried by them sothat the area of negative pressure is temporarily blocked, effectivelyreleasing the seeds 101 from the distal ends of the elongate hollowstructures 106. Thus, the seeds 101 are singluated along the conveyorbelt 110. In various embodiments, the rotating drum 104 may have asingle radial pattern of elongate hollow structures 106, or, as shown inthe figure, it may have a series of elongate hollow structures 106arranged in a radial pattern.

A vision system 114 and sorting system 115 are shown downstream from therotating drum. As noted above, the vision system 114 comprises anilluminating device, at least one sensing device, and a controllerconfigured to control the illuminating and sensing devices. In theexemplary embodiment, the illuminating device comprises a light sourcethat uses a bulb configured to emit light at a wavelength spectrummatched to illuminate the fluorescent protein marker. The exemplaryembodiment includes multiple CCD cameras and filters configured toenhance the illumination and to aid in discerning the presence of themarker. The seeds 101 are sorted by the sorting system into “+”containers 116 and “−” containers 118. In the exemplary embodiment, aseries of mechanical deflectors and/or valves (see element 55, FIG. 8,for example) are used to sort the pattern of singulated seeds based onthe presence or absence of the marker. The seeds containing the markerare sorted into the “+” containers 116; the seeds that do not containthe marker are sorted into the “−” containers 118. Although not shown inthe figure, in other embodiments the seeds contained in the “−”container 118 may be re-routed through the hopper 102 so that theseseeds make a successive pass through the system 100. In such a mannerany seeds that were not identified as exhibiting the marker may beidentified in one or more successive passes through the system 100.

FIG. 4 shows another exemplary embodiment of a singulating, evaluating,and sorting system 200 employing a method in accordance with oneembodiment of the present invention. In the exemplary embodiment, avibratory stepped bowl 202 is configured to singulate seeds from a bulksample A and pass the singulated seeds 201 through an exit aperture 206which may be located, for example, near an upper periphery of thestepped bowl 202 of the system 200. For example, in some embodiments,the system may include a commercially-available seed counter (such asthe Seedburo 801 Count-A-Pak™ vibratory counter device manufactured bySeedburo Equipment Company in Chicago, Ill.). In such embodiments, theseeds 201 of the bulk sample A may be loaded into the stepped bowl 202of the system 200 such that as the stepped bowl 202 is vibrated, theseeds 201 may be lined up in single file along a periphery of the tracks204 defined on the steps of the stepped bowl 202 and advanced toward theexit aperture 206 and out through an exit chute 207 onto a conveyor belt210. As noted above, the conveyor belt 210 is driven by rotating drivingmembers 212 that drive the conveyor belt 210 in the direction shown. Invarious embodiments, the speed of the driving members 212 may beadjusted to optimize downstream evaluating and sorting of the seeds 201.

A vision system 214 and sorting system 215 are shown downstream from thebowl 202. As noted above, the vision system 214 comprises anilluminating device, at least one sensing device, and a controllerconfigured to control the illuminating and sensing devices. In theexemplary embodiment, the illuminating device comprises a light sourcethat uses a bulb configured to emit light at a wavelength spectrummatched to illuminate the fluorescent protein marker. One exemplaryembodiment includes multiple CCD cameras and filters configured toenhance the illumination and to aid in discerning the presence of themarker. The seeds 201 are sorted by the sorting system 215 into “+”containers 216 and “−” containers 218. In the exemplary embodiment, aseries of mechanical deflectors are used to the singulated seeds 201based on the presence or absence of the marker. In the exemplaryembodiment, seeds containing the marker are sorted into the “+”containers 216 and seeds that do not contain the marker are sorted intothe “−” containers 218. Although not shown in the figure, in otherembodiments the seeds 201 contained in the “−” container 218 may bere-routed through the hopper 202 so that these seeds make a successivepass through the system 200. In such a manner any seeds that were notidentified as exhibiting the marker may be identified in one or moresuccessive passes through the system 200.

FIG. 5 shows another exemplary system 300 for singulating, evaluating,and sorting seeds based on the presence or absence of a marker inaccordance with an embodiment of the present invention. The exemplaryembodiment includes a hopper 302 that receives a bulk sample A of seedsand feeds the seeds onto a disk 304. In the exemplary embodiment, thehopper 302 includes a gate 303 that allows a controlled release of aquantity of seeds 301 onto the disk 304 based on gravitational force.The disk 304 is operatively connected to a motor (not shown) through ashaft 305 such that the disk 304 rotates in the direction shown. Thedisk 304 also includes a series of seed gates 308 that are located alonga periphery 306 of the disk 304. The seed gates 308 are configured toreceive individual seeds 301 that have been forced toward the periphery306 of the disk 304 due to centrifugal force caused by the rotation ofthe disk 304. In the exemplary embodiment, the gates 308 arecontrollable such that each gate 308 may open to release individualseeds 301. An exit chute 307 is located adjacent the periphery 306 ofthe disk 304. In the exemplary embodiment, each gate 308 may beindividually controlled to open and release an individual seed 301 whenthe gate 308 is adjacent the exit chute 307. A seed 301 released by agate 308 when adjacent the exit chute 307 travels through the exit chute307 and is deposited onto a conveyor belt 310. As noted above, theconveyor belt 310 is driven by rotating driving members 312 that drivethe conveyor belt 310 in the direction shown. In various embodiments,the speed of the driving members 312 may be adjusted to optimizedownstream evaluating and sorting of the seeds 301. As a result, seeds301 are singulated along the conveyor belt 310. As similarly describedabove, a vision system 314 and sorting system 315 are shown downstreamfrom the rotating disk 304 for evaluating and sorting seeds 301 based onthe presence or absence of the marker.

FIG. 6 shows yet another exemplary system 400 for singulating,evaluating, and sorting seeds based on the presence or absence of themarker in accordance with an exemplary embodiment of the presentinvention. In the exemplary embodiment, a hopper 402 is configured toreceive a bulk sample A of seeds. The hopper 402 may be vibrating andmay include a forward pitch that leads to an opening 403 such that seedsfrom the bulk sample A leave the opening 403 at a controlled rate. Asloped device 404 is located adjacent the opening 403 of the hopper 402.The sloped device include a first end 405 that is located adjacent theopening 403 of the hopper 402, and a second end 407 that is located alower elevation than the first end 405. The sloped device of theexemplary embodiment includes at least one groove 406 configured to forma channel that aligns seeds exiting the hopper 402 into a single filerow of individual seeds 401. In the exemplary embodiment, the groove 406is v-shaped, however in other embodiments the groove 406 may be anyother shape, such as u-shaped, that is configured to align seeds into asingle file row of individual seeds 401. Seeds 401 aligned in the groove406 of the sloped device 404 are urged toward the second end 407 of thesloped device 404 by gravitational force. A conveyor belt 410 is locatedbelow the second end 407 of the sloped device 404 to receive individualseeds 401 that fall by force of gravity from the second end 407 of thesloped device 404. As noted above, the conveyor belt 410 includesrotating driving members 412 that drive the conveyor belt 410 in thedirection shown. In various embodiments, the speed of the drivingmembers 412 may be adjusted to optimize downstream evaluating andsorting of the seeds 401. As a result, seeds 401 are singulated alongthe conveyor belt 410. As similarly described above, although not shown,a vision system and sorting system (see FIG. 8, for example) are locateddownstream from the sloped device for evaluating and sorting seeds basedon the presence or absence of the marker. As described in theExperimental Example herein, a vibratory hopper 402 singulation device,coupled with a Satake ScanMaster® sorting system may result inrelatively efficient and accurate sorting results. For example, usingsuch an exemplary system, the sorting step 16 may comprises sorting theseeds at a speed of at least about 500 seeds per minute, and in someembodiments at a speed of at least about 750 seeds per minute.

The foregoing merely illustrates how exemplary embodiments of thepresent invention distinguish seeds containing a genetic element ofinterest from a bulk sample. Referring now to FIG. 7, a block diagram ofan exemplary electronic device (e.g., PC, laptop, PDA, etc.) configuredto execute the method of distinguishing seeds containing a geneticelement of interest of exemplary embodiments of the present invention isshown. The electronic device may include various means for performingone or more functions in accordance with exemplary embodiments of thepresent invention, including those more particularly shown and describedherein. It should be understood, however, that the electronic device mayinclude alternative means for performing one or more like functions,without departing from the spirit and scope of the present invention. Asshown, the electronic device may generally include means, such as aprocessor, controller, or the like 740 connected to a memory 742, forperforming or controlling the various functions of the entity.

The memory can comprise volatile and/or non-volatile memory, andtypically stores content, data or the like. For example, the memorytypically stores content transmitted from, and/or received by, theelectronic device. Also for example, the memory typically storessoftware applications, instructions or the like for the processor toperform steps associated with operation of the electronic device inaccordance with embodiments of the present invention. In particular, thememory 742 may store computer program code for an application and othercomputer programs. For example, in one exemplary embodiment of thepresent invention, the memory may store computer program code for, amongother things, evaluating at least some of the seeds of a bulk sample forthe presence or absence of a marker associated with at least some seedscontaining a genetic element of interest of the bulk sample using anevaluating device, and sorting the seeds containing a genetic element ofinterest based on the presence or absence of the marker.

In addition to the memory 742, the processor 740 can also be connectedto at least one interface or other means for displaying, transmittingand/or receiving data, content or the like. In this regard, theinterface(s) can include at least one communication interface 746 orother means for transmitting and/or receiving data, content or the like,as well as at least one user interface that can include a display 748and/or a user input interface 750. The user input interface, in turn,can comprise any of a number of devices allowing the electronic deviceto receive data from a user, such as a keypad, a touch display, ajoystick or other input device.

As described above and as will be appreciated by one skilled in the art,embodiments of the present invention may be configured as a method andapparatus. Accordingly, embodiments of the present invention may becomprised of various means including entirely of hardware, entirely ofsoftware, or any combination of software and hardware. Furthermore,embodiments of the present invention may take the form of a computerprogram product consisting of a computer-readable storage medium (e.g.,the memory 742 of FIG. 16) and computer-readable program instructions(e.g., computer software) stored in the storage medium. Any suitablecomputer-readable storage medium may be utilized including hard disks,CD-ROMs, optical storage devices, or magnetic storage devices.

Exemplary embodiments of the present invention have been described abovewith reference to block diagrams and flowchart illustrations of methods,apparatuses (i.e., systems) and computer program products. It will beunderstood that each block of the block diagrams and flowchartillustrations, and combinations of blocks in the block diagrams andflowchart illustrations, respectively, can be implemented by variousmeans including computer program instructions. These computer programinstructions may be loaded onto a general purpose computer, specialpurpose computer, or other programmable data processing apparatus toproduce a machine, such that the instructions which execute on thecomputer or other programmable data processing apparatus create a meansfor implementing the functions specified in the flowchart block orblocks.

These computer program instructions may also be stored in acomputer-readable memory that can direct a computer or otherprogrammable data processing apparatus to function in a particularmanner, such that the instructions stored in the computer-readablememory produce an article of manufacture including computer-readableinstructions for implementing the function specified in the flowchartblock or blocks. The computer program instructions may also be loadedonto a computer or other programmable data processing apparatus to causea series of operational steps to be performed on the computer or otherprogrammable apparatus to produce a computer-implemented process suchthat the instructions that execute on the computer or other programmableapparatus provide steps for implementing the functions specified in theflowchart block or blocks.

Accordingly, blocks of the block diagrams and flowchart illustrationssupport combinations of means for performing the specified functions,combinations of steps for performing the specified functions and programinstruction means for performing the specified functions. It will alsobe understood that each block of the block diagrams and flowchartillustrations, and combinations of blocks in the block diagrams andflowchart illustrations, can be implemented by special purposehardware-based computer systems that perform the specified functions orsteps, or combinations of special purpose hardware and computerinstructions.

The following Experimental Example is provided only by way of example,and not by way of limitation.

EXPERIMENTAL EXAMPLE

Introduction

Fluorescent protein (FP) marked seed are being produced for use insterility systems and for evaluating the impact of one or more insertedgenes on yield. It is a laborious process to separate a segregatingpopulation of seed into those containing (+) and those not containing(−) a genetic element of interest.

A project was initiated to develop an automated sorting routine that maybe capable of efficiently separating FP+ from FP− seed using a vibratoryfeeder similar to that shown in FIG. 6

Results

A vibratory feeder (see FIG. 6, for example) was evaluated with theSatake ScanMaster® system to assess sorting speed and accuracy in someembodiments of the present invention. It is known that it takesapproximately 30 minutes to sort 3500 kernels by hand. The FP-discerningScanMaster® (see FIG. 8, for example) equipped with a vibratory feeder(see FIG. 6, for example) for singulation, was shown to be capable ofsorting the same sample in about 2 to 3 minutes. Thus, the substantiallyautomated method embodiments of the present invention reduced sortingtime by approximately 90%. Unfortunately, the ScanMaster® color sorterwas only able to remove 90 to 95% of the FP seed from a 50:50 mixture ina single pass. During this process a significant number of FP− seed werecommingled with FP+ seed in what should be a pure FP+ sample. This levelof performance then suggests that some manual sorting may be required insome method embodiments to achieve a desired level of purity.

For example, if a typical yield trial sample contained 4000 kernels (50%FP− and 50% FP+) it would require about 40 minutes to sort the FP seed.This is a sorting rate of 50 seeds/minute. If the same sample weresorted using substantially automated embodiments of the presentinvention, it would require less than 30 seconds to generate a 95% puresample of FP+ seed. For a 2000 kernel FP+ sample, there would be about100 FP− kernels that would need to be manually removed. If the manualsorting rate is 50 seeds/minute, the actual time to achieve a nearly100% pure sample of FP+ seed will be about 2 minutes. Furthermore, if asample is manually sorted while another is being sorted using the FPSorter the actual sorting time for a sample would be about 2 minutes.This results in a fifteen-fold reduction in time required for separatingFP+ seed from FP− seed.

If an automatic re-sort function (i.e. re-routing the sample backthrough the sorting procedure for one or more additional passes) isused, it may be possible to recover 99% of the FP+ seed from the initialsample without having to manually re-sort the FP− fraction. Such are-sort process extends the cycle time by 15 seconds for a 500 gram seedsample. Given that it will take 2 minutes to sort the FP+ fraction itmay be advantageous to routinely re-sort samples, especially small ones,to recover as much of the FP+ seed as possible.

As noted above, the expression of fluorescent proteins may benon-uniform across the surface area of seeds. As a result, the presentinvention also provides a method for distinguishing seeds containing amarker associated with genetic element of interest from a bulk sample byusing an photonic emitting device that is configured to excite amajority of the surface area of the seeds and/or by using an evaluatingdevice that is configured receive emissions from a majority of thesurface area of the seeds. FIG. 9 shows a non-limiting schematic of asystem incorporating a vacuum drum singulating device, an photonicemitting device, and an evaluating device in accordance with oneembodiment of the present invention. Specifically, FIG. 9 shows a system500 that includes an exemplary embodiment of a singulating devicecomprising a plurality of elongate hollow structures operativelyconnected to a vacuum source used to singulate seeds from a bulk sample.Specifically, the system 500 of the exemplary embodiment includes ahopper 502 into which a bulk sample A of seeds may be placed. A rotatingdrum 504 is positioned adjacent the hopper 502. The rotating drum 504includes a plurality of elongate hollow structures 506 that extend intoa substantially hollow interior of the drum 504, which is connected to avacuum source (not shown). The vacuum source creates a zone of negativepressure within the interior of the drum 504, and as a result, distalends of the elongate hollow structures 506 create discrete areas ofnegative pressure. As shown in the figure, the drum 504 rotates adjacentan open end of the hopper 502. The hopper 502 is configured such thatseeds are urged toward the open end and adjacent the rotating drum 504.The drum 504 rotates in the direction shown such that the elongatehollow structures 506 pass through a portion of the seeds of the bulksample A adjacent the drum 504.

As the elongate hollow structures 506 rotate through the bulk sample A,the discrete areas of negative pressure located at the distal ends ofthe elongate hollow structures 506 attract individual seeds 501. Thesize of the distal ends of each of the elongate hollow structures 506 isconfigured such the discrete area of negative pressure at the distal endof each of the hollow structures 506 attracts a single seed 501. Asshown in the figure, as the elongate hollow structures 506 rotatethrough the open end of the hopper 502, individual seeds 501 attach tothe distal ends of the elongate hollow structures 506. As the drum 504continues to rotate in the direction shown, a deflector plate 508 (oralternatively, in some embodiments, a compressed air source configuredfor detaching individual seeds from the elongate hollow structures 506)deflects the seeds 501 from the distal ends of the elongate hollowstructures 506 and onto the conveyor belt 510. In the exemplaryembodiment, the deflector plate 508 contacts between the distal ends ofthe elongate hollow structures 506 and the seeds 501 carried by them sothat the area of negative pressure is temporarily blocked, effectivelyreleasing the seeds 501 from the distal ends of the elongate hollowstructures 506.

As shown generally in FIG. 9, the system 500 may also include aspecialized vision system 554 which, in some embodiments, may comprise:(1) an photonic emitting device, such as an illuminating device 554 athat emits light at a particular wavelength chosen to illuminate andthereby “excite” a marker, and (2) an evaluating device, such as animage sensing device 554 c that may discern seeds expressing the marker.In various embodiments, the present invention may include anelectronmagnetic energy emitting device that is configured to excite amajority of the surface area of the seeds and/or an evaluating devicethat is configured to receive emissions from a majority of the surfacearea of the seeds. In the depicted embodiment, the system 500 includes apair of illuminating devices 554 c collectively configured to excite amajority of the surface area of the seeds. In such a manner, the imagesensing device 554 c may evaluate a majority of the surface area of theseeds to determine the presence or absence of a marker.

In the depicted embodiment, image sensing device 554 c may be furtherconfigured for translating the emission into substantially “white”light. Thus, the image sensing device may assign substantially binaryvalues to each seed based on the presence or absence of the markerwherein seeds containing a genetic element of interest (tagged with therelatively “bright” marker) are marked “positive” (and thereby deflectedand/or other wise directed into one or more “+” containers 556. Seedsthat do not contain a genetic element of interest, or other particulatedebris (which may be translated into a “dark” or “negative” result) maybe dropped and/or otherwise directed into one or more “−” containers558. As shown in FIG. 9, the image sensing device 554 c (or othercomponent of a vision system 554 may be in communication with thedeflector plate 508, which may also include a guide plate 565 that mayrotate for directing the “positive” (i.e. seeds containing a geneticelement of interest (which the image sensing device 554 c may detect as“white” or “bright” seeds)) into one or more “+” containers 556 inresponse to a binary positive or “1” signal received from the imagesensing device 554 c or other processing component of the vision system554. The guide plate 565 may also be configured for directing the“negative” (i.e. seeds that do not contain a genetic element of interestor particulate debris (which the image sensing device 554 c may detectas “dark” seeds)) into one or more “−” containers 558 in response to abinary negative or “0” signal received from the image sensing device 554c or other processing component of the vision system 554.

Many different configurations are possible for distinguishing seedscontaining a marker associated with genetic element of interest from abulk sample by using an photonic emitting device that is configured toexcite a majority of the surface area of the seeds and/or by using anevaluating device that is configured receive emissions from a majorityof the surface area of the seeds. Another non-limiting example is showngenerally in FIG. 10, which depicts a sorting system 600 that includes aspecialized vision system 654 which, in some embodiments, may comprise:(1) an photonic emitting device, such as an illuminating device 654 a,that emits light at a particular wavelength chosen to illuminate andthereby “excite” a marker, and (2) an evaluating device, such as animage sensing device 654 c that may discern seeds expressing the marker.In the depicted embodiment, the system 600 includes a pair ofilluminating devices 654 a configured to collectively excite a majorityof the surface area of the seeds and a pair of image sensing devices 654c configured to collectively receive emissions from a majority of thesurface area of the seeds. In such a manner, the image sensing device654 c may evaluate a majority of the surface area of the seeds todetermine the presence or absence of a marker.

As similarly described above, the evaluating device 654 c of FIG. 10 (orother component of a vision system 654) may be in communication with asorting device 655 (which may comprise, for example, a valve deviceand/or compressed air jet device) configured for directing the“positive” (i.e. seeds containing a genetic element of interest (whichthe image sensing device 654 c may detect as “white” or “bright” seeds))into one or more “+” containers 656 in response to a binary positive or“1” signal received from the image sensing device 654 c or otherprocessing component of the vision system 654. The sorting device 655may also be configured for directing the “negative” (i.e. seeds that donot contain a genetic element of interest or particulate debris (whichthe image sensing device 654 c may detect as “dark” seeds)) into one ormore “−” containers 658 in response to a binary negative or “0” signalreceived from the image sensing device 654 c or other processingcomponent of the vision system 654.

FIG. 11 shows an evaluating device 700 in accordance with anotherembodiment of the present invention wherein a fluorescent protein markerhas been associated with at least some seeds of a bulk sample. Invarious embodiments, the evaluating device 700 is configured to beportable and may be moved to various sorting locations. In the depictedembodiment, the evaluating device 700 comprises a portable table-topdevice that includes an open-faced enclosure. In the depictedembodiment, samples of seeds 701 from the bulk sample may be collectedand placed into an evaluating area 703 within the open-faced enclosureof the evaluating device 700 for evaluating the samples of seeds 701based on the presence or absence of the fluorescent maker. In variousembodiments, the evaluating area 703 of the evaluating device 700 may beconfigured such that seeds 701 placed in the evaluating area 703 may beexcited by one or more light sources 705. Although in variousembodiments a variety of fluorescent markers may be used, in thedepicted embodiment an RFP marker is associated with at least some seedsfrom the bulk seed sample that contain a genetic element of interest.Also, although in various embodiments a variety of light sources may beused to excite samples of seeds from the bulk sample, in the depictedembodiment the seed samples are excited by a pair of laboratory ratedcold light sources, in particular a pair of Model KL 2500 LCD fiberoptic light sources that have the capacity for multiple fluorescenceexcitation filters, available from Schott Corporation of Elmsford, N.Y.In the depicted embodiment, the light sources 705 include respectivegooseneck guides 709. The enclosure of the device 700 is configured toreceive the guides 709 so as to illuminate at least a portion of theevaluating area 703.

In the depicted embodiment, either or both of the light sources 705 areconfigured to excite samples of seeds 701 from the bulk seed sample suchthat the seed samples may be inspected and sorted based on the presenceor absence of the RFP marker. In the depicted embodiment, the seeds 701are inspected by viewing the seeds 701 in the evaluating area 703through a filter 707 that is integrated into the evaluating device 700.Although in various embodiments the filter 707 may comprise any one orany combination of filters, in the depicted embodiment the filter 707comprises a red band pass optical filter. It should be noted that inother embodiments, the samples of seeds 701 may be inspected and sortedusing other filtering devices, including, for example, filtered eyewearsuch as glasses or goggles configured to be worn by an operator. Anexample of such filtered eyewear used by an operator to inspect and sortseeds based on the presence or absence of an RFP marker are Red LaserEnhancement Glasses, available from W.W. Grainger, Inc. of Lake Forest,Ill. It should also be noted that in some embodiments, a magnifying lensmay be used to aid an operator in inspecting the seeds 701. In variousembodiments, the magnifying lens may be part of the evaluating device700, or it may be an independent device. For example, in someembodiments magnifying lenses may be included in eyewear configured tobe worn by an operator.

In any event, the seeds are then sorted by the operator based on thepresence or absence of the red fluorescent protein, the presence ofwhich is manifested by glowing (or fluorescing) proteins that arevisible to the operator. Although in various other embodiments, theoperator may sort the seeds in any manner, in the depicted embodiment,the evaluating device 700 includes a pair of sorting funnels 711 thatlead to a pair of respective containers 713. In such a manner, theoperator may sort the seeds based on the presence or absence of the redfluorescent protein by directing the respective seeds into thecontainers 713.

As such, the evaluating device 700 of the depicted embodiment allows fora high degree of accuracy in identifying and sorting seeds that do or donot contain a genetic element of interest based on the presence orabsence of the fluorescent marker. As such the need for seeds to bere-evaluated through multiple seed sorting passes is greatly reduced orsubstantially eliminated.

FIG. 12 shows another system 800 for evaluating and sorting seeds basedon the presence or absence of a marker in accordance with anotherembodiment of the present invention. In the depicted embodiment, a seedfeeding apparatus 801 is shown that includes a hopper 802, a seedfeeding tray 803, and a vibration generating apparatus 805 configured tovibrate the tray 803 and/or the hopper 802. A suitable feeding apparatusis available from Magnetic Products, Inc. of Highland, Mich. as theVibratory Feeder Hopper “VFH” series.

Although in various embodiments a variety of fluorescent markers may beused, in the depicted embodiment an RFP marker is associated with atleast some seeds from the bulk seed sample that contain a geneticelement of interest. Also, although in various embodiments a variety oflight sources may be used to excite samples of seeds from the bulksample, in the depicted embodiment the seed samples are excited with anLED (light-emitting diode) light source, specifically a green(approximately 490 nm to 560 nm, and, in the depicted embodiment,approximately 530 nm) LED light source. In some embodiments, the greenLED light source may comprise a green LED array light source. Examplesof suitable green LED array light sources are available from BannerEngineering Corporation of Plymouth, Minn.

In the depicted embodiment, the hopper 802 of the seed feeding apparatus801 is configured to receive a bulk sample A of seeds. The hopper 802may be vibrating and may include a forward pitch that leads to anopening such that seeds from the bulk sample A leave the opening ontothe seed feeding tray 803. In the depicted embodiment, the seed feedingtray 803 is vibrated by the vibration generating apparatus 805 such thatseeds move along the length of the seed feeding tray 803. In variousembodiments, the speed at which the seeds travel along the seed feedingtray 803 may be adjustable, such as by adjusting parameters of thevibration generating apparatus and/or parameters of the seed feedingtray 803 itself. The LED light source 808 is located above a portion ofthe seed feeding tray 803 such that the LED light source 808 excites atleast a portion of the seeds 801 on the seed feeding tray 803. Althoughin other embodiments, the excited seeds 801 may be inspected and sortedin various ways, in the depicted embodiment the excited seeds 801 aremanually inspected by one or more operators wearing filtering eyewear810. In the depicted embodiment, the one or more operators wear red bandpass filtered glasses to inspect and sort the excited seeds 801. Anexample of such eyewear used by an operator to inspect and sort seedsbased on the presence or absence of an RFP marker are Red LaserEnhancement Glasses, available from W.W. Grainger, Inc. of Lake Forest,Ill. The seeds are then sorted by the operator based on the presence orabsence of the red fluorescent protein, the presence of which ismanifested by glowing (or fluorescing) proteins that are visible to theoperator. Although in various embodiments, the seeds may be separated invariety of ways, in the depicted embodiment, a container 811 is placedbelow the downstream end of the seed feeding tray 803. In such a manner,the seeds are separated by the operator based on the presence or absenceof the RFP marker. In the depicted embodiment, seeds expressing the RFPmarker are collected by the operator while seeds not expressing the RFPmarker (i.e., the non-fluorescing seeds) continue to travel along theseed feeing tray 803 until they fall into the container 811.

As such, the evaluating device 800 of the depicted embodiment allows fora high degree of accuracy in identifying and sorting seeds that do or donot contain a genetic element of interest based on the presence orabsence of the fluorescent marker. As such the need for seeds to bere-evaluated through multiple seed sorting passes may be greatly reducedor substantially eliminated.

FIG. 13 shows a schematic representation of another exemplary system 900that may be used to distinguish seeds containing a genetic element ofinterest from a bulk sample of seeds in accordance with one exemplaryembodiment. In the exemplary embodiment, the system 900 is a modifiedcommercially available seed sorter, such as a modified version of aSatake ScanMaster® sorting system available from Satake-USA of Stafford,Tex.

In the depicted embodiment, a bulk sample A of seeds are loaded into ahopper 952. Although in various embodiments a variety of fluorescentmarkers may be used, in the depicted embodiment an RFP marker isassociated with at least some seeds from the bulk seed sample thatcontain a genetic element of interest. The hopper 952 is configured tofunnel the bulk sample A of seeds into separate chutes 953 that aresized to accommodate a particular volume for processing by a visionsystem 954. The seeds from each chute 953 fall by force of gravity pastthe vision system 954. In the exemplary embodiment, the vision system954 comprises an illuminating device 957, at least one sensing device,and a controller configured to control the illuminating and sensingdevices.

Although in various embodiments a variety of light sources may be usedto excite samples of seeds from the bulk sample, in the depictedembodiment the illuminating device 957 comprises an LED light source,specifically a green (approximately 490 nm to 560 nm, and, in thedepicted embodiment, approximately 530 nm) LED array light source.Because of the high speed application of the depicted embodiment, an LEDlight source may be preferable to another light source, such as afluorescent light source because the light from the fluorescent lightsource may vary depending on the manufacturing quality and age of thesystem. Additionally, the environment in which the system operates maynegatively affect a fluorescent light source. In the depictedembodiment, an LED light source may be advantageous because it producesrepeatable light output with minimal variations generated by thesurrounding environment. Examples of suitable green LED array lightsources are available from Banner Engineering Corporation of Plymouth,Minn.

The exemplary embodiment includes multiple CCD cameras with filters(i.e. red band pass filters) configured to enhance the illumination andto aid in discerning the presence of the RFP marker. Although otherembodiments may use fewer cameras, the exemplary embodiment allows seedsfalling past the vision system 954 to be viewed from the front and back.In other embodiments, any vision system 954 configured to discern thepresence of a RFP marker may be used, including, but not limited to, CCDdevices, CMOS devices and other vision sensors.

In the depicted embodiment, the sorting function is carried out by asorting device 955, which comprises a number of individual pneumaticejectors that emit a controlled blast of air (such as an “air knife” forexample) configured for sorting seeds that exhibit the RFP marker as theseeds pass through the sorting device. Seeds exhibiting the RFP markerare sorted into containers 956, identified in the figure with a “+”symbol. Seeds that do not contain the marker fall into containers 958,identified in the figure with a “−” symbol. Although not shown in thefigure, in other embodiments the seeds contained in the “−” container958 may be re-routed through the hopper 952 so that these seeds make asuccessive pass through the system 950. In such a manner any seeds thatwere not identified as exhibiting the marker may be identified in one ormore successive passes through the system 900.

In such a manner, the system 900 of the depicted embodiment allows for ahigh degree of accuracy in identifying and sorting seeds that do or donot contain a genetic element of interest based on the presence orabsence of the fluorescent marker. As such the need for seeds to bere-evaluated through multiple seed sorting passes may be greatly reducedor eliminated.

The above described method allows the processing of a large quantity ofseeds, a portion of which include a marker that is associated with agenetically transformed seed including a desired trait. However in otherembodiments, a bulk sample may include various seeds having differentmarkers associated with different desired traits, or seeds that includemore than one marker associated with different desired traits.

Many modifications and other embodiments of the invention set forthherein will come to mind to one skilled in the art to which thisinvention pertains having the benefit of the teachings presented in theforegoing descriptions and the associated drawings. Therefore, it is tobe understood that the invention is not to be limited to the specificembodiments disclosed and that modifications and other embodiments areintended to be included within the scope of the appended claims.Although specific terms are employed herein, they are used in a genericand descriptive sense only and not for purposes of limitation.

What is claimed is:
 1. A method for distinguishing seeds containing agenetic element of interest from a bulk sample of seeds, the methodcomprising: associating a fluorescent protein marker with a geneticelement of interest contained in at least some of the seeds of a bulksample; exciting fluorescence in at least some of the seeds in the bulksample with an LED light source; automatically feeding the bulk sampleof seeds past an image sensing device; and automatically sorting theseeds based on the presence or absence of fluorescence.
 2. The method ofclaim 1, wherein exciting at least some of seeds with an LED lightsource comprises exciting at least some of the seeds with an LED array.3. The method of claim 1, wherein exciting at least some of the seedswith an LED light source comprises exciting at least some of the seedswith a green LED light source.
 4. The method of claim 1, whereinexciting at least some of the seeds with an LED light source comprisesexciting at least some of the seeds with a green LED array light source.5. The method of claim 1, wherein the seeds are placed into a hopperprior to being fed past an image sensing device.
 6. The method of claim5, wherein fluorescence is excited after the seeds are placed in thehopper.
 7. The method of claim 1, wherein the seeds are singulated priorto being fed past an image sensing device.